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Clinical Trial Details
Microbiota, Metabolites and Colon Neoplasia
Clinical Trial ( IRB ) #: 21-167JSO-1
Title: Microbiota, Metabolites and Colon Neoplasia
Principal Investigator: Dr. Daniel Rosenberg
Description: Dr. Daniel W. Rosenberg and his project Co-Investigators are conducting a research study called "Microbiota, Metabolites, and Colon Neoplasia" to examine whether eating walnuts can have a beneficial effect on the gut bacteria population, inflammatory markers in the blood, and the tissue that lines the inside of the colon. This is a 29-day dietary intervention study where participants will be asked to consume 2 ounces of walnuts daily for 21 days, and at the end of the study period they will come in for a routine colonoscopy. After being informed about the study and potential risks, participants giving written informed consent will first start a 7-day wash-out period where they will be asked to avoid foods high in ellagitannins (ET) for the duration of the study. In addition, participants will be asked to complete food and activity questionnaires, a walnut consumption log, and two sets of 3-day dietary records during their participation in the study. Participants will also be asked to provide three urine samples, two blood samples, and two stool samples at multiple time points, and 8-10 colon tissue specimens (biopsies) will be collected during their colonoscopy procedure for the purposes of this study.
Classification:
  Cancer - Gastrointestinal
  Cancer - Prevention
  Gastrointestinal (Stomach, Bowel, Etc.)
Eligibility Criteria: INCLUSION 1. Men & women in one of the following groups: A) Between the ages of 40-75 years old, who are scheduled to undergo a routine screening or surveillance colonoscopy for colorectal cancer (CRC) and have a family history of CRC in a first-degree relative diagnosed with CRC under the age of 65 years, or B) Between the ages of 45-75 years old, who are referred for colonoscopy following a positive fecal immunochemical test (FIT) and have not had a high quality colonoscopy in the past 3 years 2. Willing and able to provide written informed consent for study participation 3. Willing to consume 2 ounces (56 grams) of walnuts daily for 3 weeks 4. Willing to avoid intake of ET-rich foods and beverages (e.g., pomegranates, hazelnuts, pistachios, strawberries, raspberries, blackberries, oak-aged wines, and other food on a list given by researchers) and fermented dairy products containing viable Bifidobacteria or Lactobacilli) 5. Willing to stop taking dietary supplements, including probiotics 6. Willing to have two separate blood draws, as well as urine and stool collections 7. Willing to comply with all study requirements EXCLUSION 1. Personal history of CRC, or a history of any malignancy (other than skin cancer) within the past 5 years 2. Individual meets the Amsterdam criteria for Lynch Syndrome or has a history of familial adenomatous polyposis (FAP) 3. Individual has been treated with immunosuppressive agents or systemic steroids, excluding inhalers, within two weeks prior to the Screening Visit and for the duration of the study 4. Use of antibiotics within one month prior to the Screening Visit and for the duration of the study 5. Individuals with severe medical illness or those at high risk for anesthesia 6. Current evidence or previous history of ulcerative colitis or Crohn’s disease 7. Colonoscopy performed for reasons other than screening or surveillance for CRC 8. HIV infection, chronic viral hepatitis 9. Allergy to walnuts or hypersensitivity to tree nuts 10. Peri-menopausal women with any chance or plan of pregnancy 11. Individuals with blood coagulation disorders or on anti-coagulant therapy 12. Individuals residing in the Department of Correction 13. Any other condition that, in the opinion of the PI, might interfere with study objectives
How to Contact: Amy Pallotti. Telephone: 860-679-3878. Email: apallotti@uchc.edu
Enrollment Status/Comments: Enrollment status: Enrolling/recruiting. For current recruitment status, please check with study contact. Comments: A total of 200 subjects will be enrolled across two sites (UConn Health and Weill Cornell Medicine).